Investig Clin Urol.  2019 Nov;60(6):447-453. 10.4111/icu.2019.60.6.447.

Clinical significance of the De Ritis ratio for detecting prostate cancer in a repeat prostate biopsy

Affiliations
  • 1Department of Urology, Kyungpook National University Hospital, Daegu, Korea. uroyoo@knu.ac.kr
  • 2Department of Urology, Kyungpook National University Chilgok Hospital, Daegu, Korea.
  • 3Department of Urology, School of Medicine, Kyungpook National University, Daegu, Korea.
  • 4Department of Pathology, Kyungpook National University Chilgok Hospital, Daegu, Korea.

Abstract

PURPOSE
We evaluated factors predicting a positive repeat biopsy result in patients with an initial negative prostate biopsy result.
MATERIALS AND METHODS
This study included 124 patients in whom prostate cancer (PCa) was not detected in the initial transrectal ultrasound-guided prostate biopsy and who underwent repeat biopsy from January 2011 to December 2017. Patients without PCa in both initial and repeat prostate biopsies were designated as group 1 (n=82), and those in whom PCa was detected on a repeat prostate biopsy were designated as group 2 (n=42). Among group 2 patients, 6 had insignificant PCa according to the Epstein criteria and were combined with group 1 patients to make up group A (n=88). Patients with significant PCa were categorized as group B (n=36). We compared clinicopathologic characteristics between the groups.
RESULTS
Multivariate analysis showed that age (p=0.018) and detection of atypical small acinar proliferation (ASAP) or ≥3 cores of high-grade prostatic intraepithelial neoplasia (HGPIN) (p=0.011) on the initial biopsy were predictive factors for a positive result on a repeat biopsy. When we compared group A and group B, age (p=0.004) and the De Ritis ratio (p=0.024) were significantly higher in group B in the multivariate analysis.
CONCLUSIONS
Age and the detection of ASAP or ≥3 cores of HGPIN on the initial biopsy were associated with detection of PCa on a repeat biopsy. Age and the De Ritis ratio were found to be predictive factors for the detection of clinically significant PCa on a repeat biopsy.

Keyword

Biopsy; Prostatic neoplasms; Transaminases

MeSH Terms

Biopsy*
Humans
Multivariate Analysis
Passive Cutaneous Anaphylaxis
Prostate*
Prostatic Intraepithelial Neoplasia
Prostatic Neoplasms*
Transaminases
Transaminases

Figure

  • Fig. 1 Study algorithm. Group 1, without prostate cancer (PCa) detection in initial and repeat prostate biopsy; group 2, PCa detected in repeat prostate biopsy; group A, benign or low-risk prostate cancer; group B, non-low-risk prostate cancer.


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